Fluid Management of Acute Decompensated Heart Failure Subjects Treated With Reprieve Decongestion Management System (DMS)
Public ClinicalTrials.gov record NCT05174312. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Fluid Management of Acute Decompensated Heart Failure Subjects Treated With Reprieve Decongestion Management System (DMS) - FASTR Trial
Study identification
- NCT ID
- NCT05174312
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Not applicable
- Lead sponsor
- Reprieve Cardiovascular, Inc
- Industry
- Enrollment
- 100 participants
Conditions and interventions
Conditions
Interventions
- Diuretic Drug
- Reprieve Decongestion Management System Device
Drug · Device
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jul 10, 2022
- Primary completion
- Jan 9, 2025
- Completion
- Jan 9, 2025
- Last update posted
- Jul 23, 2025
2022 – 2025
United States locations
- U.S. sites
- 16
- U.S. states
- 10
- U.S. cities
- 15
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Eastern Shore Research Institute | Fairhope | Alabama | 36532 | — |
| University of California Irvine | Irvine | California | 92697 | — |
| MedStar Washington Hospital Center | Washington D.C. | District of Columbia | 20010 | — |
| Trinity Health Ann Arbor Hospital | Ypsilanti | Michigan | 48197 | — |
| St. Louis VA | St Louis | Missouri | 63130 | — |
| Washington University | St Louis | Missouri | 63130 | — |
| Duke University Hospital | Durham | North Carolina | 27710 | — |
| Cone Health | Greensboro | North Carolina | 27401 | — |
| Atrium Health Wake Forest Baptist Medical Center | Winston-Salem | North Carolina | 27157 | — |
| The Lindner Research Center at Christ Hospital | Cincinnati | Ohio | 45219 | — |
| Ohio State University Hospital | Columbus | Ohio | 43210 | — |
| Medical University of South Carolina | Charleston | South Carolina | 29425 | — |
| Prisma Health | Columbia | South Carolina | 29203 | — |
| Ascension Texas Cardiovascular | Austin | Texas | 78705 | — |
| Baylor Scott & White | Dallas | Texas | 75246 | — |
| University of Vermont Medical Center | Burlington | Vermont | 05401 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT05174312, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jul 23, 2025 · Synced May 17, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT05174312 live on ClinicalTrials.gov.